Tailoring capping-layer composition for improved stability of mixed-halide perovskites
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Helmholtz-Zentrum Berlin (HZB), (Germany). German Research Centre for Materials and Energy
- Georgia Institute of Technology, Atlanta, GA (United States)
- Argonne National Lab. (ANL), Lemont, IL (United States)
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
- Florida State Univ., Tallahassee, FL (United States)
- Georgia Institute of Technology, Atlanta, GA (United States); Univ. of Colorado, Boulder, CO (United States); National Renewable Energy Lab. (NREL), Golden, CO (United States)
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Toyota Research Institute, Los Altos, CA (United States)
Incorporating a low dimensional (LD) perovskite capping layer on top of a perovskite absorber, improves the stability of perovskite solar cells (PSCs). However, in the case of mixed-halide perovskites, which can undergo halide segregation into single-halide perovskites, a systematic study of the capping layer's effect on mixed-halide perovskite absorber is still lacking. This study bridges this gap by investigating how the 1D perovskite capping layers on top of MAPb(IxBr1–x)3 (x = 0, 0.25, 0.5, 0.75, 1) absorbers affect the films' stability. We utilize a new method, dissimilarity matrix, to investigate the image-based stability performance of capping-absorber pair compositions across time. This method overcomes the challenge of analyzing various film colors due to bandgap difference in mixed-halide perovskites. We also discover that the intrinsic absorber stability plays an important role in the overall stability outcome, despite the capping layer's support. Within the 55 unique capping-absorber pairs, we observe a notable 1D perovskite material, 1-methoxynaphthalene-2-ethylammonium chloride (2MeO–NEA–Cl or 9-Cl), that improves the stability of MAPbI3 and MAPb(I0.5Br0.5)3 by at least 8 and 1.5 times, respectively, compared to bare films under elevated humidity and temperature. Surface photovoltage results also show that the accumulation of electrostatic charges on the film surface depends on the capping layer type, which could contribute to the acceleration/deceleration of degradation.
- Research Organization:
- Argonne National Lab. (ANL), Argonne, IL (United States). Center for Nanoscale Materials; Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
- Sponsoring Organization:
- Massachusetts Institute of Technology (MIT); National Science Foundation (NSF); Natural Sciences and Engineering Research Council of Canada (NSERC); Skoltech; US Air Force Office of Scientific Research (AFOSR); USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office; USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division
- Grant/Contract Number:
- AC02-06CH11357; EE0009512
- OSTI ID:
- 1886385
- Journal Information:
- Journal of Materials Chemistry. A, Journal Name: Journal of Materials Chemistry. A Journal Issue: 6 Vol. 10; ISSN 2050-7488
- Publisher:
- Royal Society of ChemistryCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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